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Trial record 30 of 2026 for:    doxil

Liposomal Doxorubicin and PSC 833 in Treating Patients With AIDS-Related Kaposi's Sarcoma or Other Advanced Cancers

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00003207
Recruitment Status : Completed
First Posted : February 16, 2004
Last Update Posted : April 12, 2013
National Cancer Institute (NCI)
Information provided by (Responsible Party):
Washington University School of Medicine

Brief Summary:

The rationale for conducting this study lies in the premise that if indeed the reason for a limited response of Kaposi's sarcoma lesions and other advanced malignancies to chemotherapy is attributable to a high expression of P-glycoprotein, then, by inhibiting this pump, tumor kill would be enhanced and response rates as well as duration of responses would also increase. Doxil is chosen since recent studies have shown that it is superior to combination chemotherapy with ABV or BV. Doxil is also known to be active in other malignancies such as breast and ovarian cancer (34,35). PSC 833 is chosen since it has been found to reverse P-gp in vitro and in vivo, is non-immunosuppressive, and has been shown in recent Phase 1 studies to be well tolerated.

There are yet no human studies reported on Doxil pharmacokinetics when combined with MDR modulators. Preclinical data shows that pharmacokinetics of Doxil, unlike free doxorubicin, is minimally affected by the addition of PSC 833 (36). Enhanced tumor toxicity was observed when PSC 833 was combined with Doxil. Since doxorubicin, the active agent in Doxil, is metabolized by the same cytochrome P450, interactions between these 2 agents may have very significant clinical implications. The purpose of this study is to assess the toxicity and determine the maximum tolerated dose of Doxil when combined with PSC 833 in the treatment of AIDS-KS and other advanced malignancies.

Condition or disease Intervention/treatment Phase
Sarcoma Unspecified Adult Solid Tumor, Protocol Specific Drug: pegylated liposomal doxorubicin hydrochloride Drug: PSC 833 Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 14 participants
Intervention Model: Single Group Assignment
Primary Purpose: Treatment
Official Title: Phase I Study on Doxil and SDZ PSC 833 in the Treatment of AIDS-Associated Kaposi's Sarcoma and Other Advanced Malignancies
Study Start Date : March 1998
Actual Primary Completion Date : July 2002
Actual Study Completion Date : July 2002

Arm Intervention/treatment
Experimental: Phase 1 (Doxil & PSC 833)
Patients will receive Doxil at the standard dose of 20 mg/m2 IV for the 1st cycle. On the 2nd cycle of Doxil, the first patient will receive Doxil at 40% of standard dose or 8 mg/m2 (dose level 1) IV over one hr. 15 mn after the 2nd and subsequent cycles of Doxil, PSC 833 will be given at 2 mg/kg for 2 hrs. Simultaneously, a 72 hour CIVI of PSC 833 will be started with the loading dose. If no DLT occurs, then a double dose escalation of Doxil (dose levels 3, 5, 7 ) will be given to the same patient in the subsequent cycles until DLT occurs. On the 2nd cycle, Doxil will be given at the next dose level above the starting dose tolerated by the first patient. If no DLT occurs, a double dose escalation will also be done for the subsequent cycles (dose levels 5, 7, 9). The single-patient-cohort will terminate when a patient experiences DLT or when two episodes of grade 2 toxicity occur. At that point patients will be enrolled into cohorts of 3 patients to determine the MTD.
Drug: pegylated liposomal doxorubicin hydrochloride
Other Name: DOXIL

Drug: PSC 833
Other Name: valspodar

Primary Outcome Measures :
  1. Safety profile and tolerability of Doxil in combination with PSC 833
    Each cycle is 2 weeks long and can continue until disease progression, toxicity, or patient decision

  2. Maximum tolerated dose of Doxil in combination with PSC 833
  3. Dose limiting toxicity of Doxil in combination with PSC 833

Secondary Outcome Measures :
  1. Effects of PSC 833 on Doxil pharmacokinetics
  2. Confirm the MDR expression with immunohistochemistry and functionally, with 99MTc-sestamibi

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No


  • Histologically documented malignancy refractory to standard treatment or for which no standard treatment exists, or biopsy proven Kaposi's sarcoma with mucocutaneous lesions numbering 10 or more or a documented visceral KS lesion with at least 2 assessable cutaneous lesions.
  • A life expectancy of >4 months.
  • Patients with prior chemotherapy and Doxil exposure are eligible
  • Age >=18
  • Karnofsky score of >=70%
  • Hemoglobin >=8 g/dl, neutrophil count >=1000 cells/ul and platelet count of >=75,000 cells/ul.
  • Creatinine clearance of .=50 ml/min or creatinine of <=2.0mg/dl, SGOT <=2X the institutional normal and bilirubin <1.5X institutional normal
  • Written informed consent has been obtained from the patient.


  • Pregnant or breast feeding patients as radioactive tracer material and chemotherapy will be used in this protocol.
  • Active opportunistic infections requiring antibiotic treatment.
  • Treatment with radiation or electron beam therapy, interferon or cytotoxic therapy within the preceding 4 weeks.
  • Clinically significant history of congestive heart failure.
  • Patients who have moderate to severe sensory and motor peripheral neuropathy.
  • Any patient currently receiving treatment with any of the following agents which cannot be discontinued at a specified time relative to PSC 833 administration. All of these drugs are well substantiated to interact with cyclosporin A:

    • Agents increasing serum concentrations of CsA

The following drugs must not be administered for 48 hours before PSC 833 is started, during the course of its administration, or up to 48 hours after the last dose of PSC 833 in a cycle:

Calcium channel blockers: diltiazem, nicardipine, verapamil Antifungals: fluconazole (dose <200 mg/day allowed), itraconazole, ketoconazole Antibiotics: clarithromycin, erythromycin Others: metoclopramide,bromocriptine, danazol

  • Agents decreasing serum concentrations of CsA

The following drugs must not be administered in the 14 days before PSC 833 is started or during the course of its administration. They may be restarted immediately after the last dose of PSC 833:

Antibiotics: nafcillin, rifampin Anticonvulsants: carbamazepine, phenobarbital, phenytoin Others: octreotide, ticlopidine

  • Hypersensitivity to Doxil or cyclosporin A
  • Any patient, who, in the judgment of the investigator, may not be able to complete this study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00003207

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United States, Missouri
Washington University School of Medicine
Saint Louis, Missouri, United States, 63110
Sponsors and Collaborators
Washington University School of Medicine
National Cancer Institute (NCI)
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Principal Investigator: Paula M. Fracasso, MD, PhD Washington University School of Medicine

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Responsible Party: Washington University School of Medicine Identifier: NCT00003207     History of Changes
Other Study ID Numbers: CDR0000066062
First Posted: February 16, 2004    Key Record Dates
Last Update Posted: April 12, 2013
Last Verified: April 2013
Keywords provided by Washington University School of Medicine:
unspecified adult solid tumor, protocol specific
AIDS-related Kaposi sarcoma
recurrent Kaposi sarcoma
Additional relevant MeSH terms:
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Liposomal doxorubicin
Sarcoma, Kaposi
Neoplasms, Connective and Soft Tissue
Neoplasms by Histologic Type
Herpesviridae Infections
DNA Virus Infections
Virus Diseases
Neoplasms, Vascular Tissue
Antibiotics, Antineoplastic
Antineoplastic Agents
Topoisomerase II Inhibitors
Topoisomerase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs